Canonical Allele Identifier: CA1217925862

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090995T= , CM000663.2:g.197090995T=	GRCh38
NC_000001.10:g.197060125T= , CM000663.1:g.197060125T=	GRCh37
NC_000001.9:g.195326748T=	NCBI36
NG_015867.1:g.60700A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2778A=
ENST00000367409.9:c.9491A= MANE Select	ENSP00000356379.4:p.Tyr3164=
ENST00000680265.1:c.9713A=	ENSP00000505384.1:p.Tyr3238=
ENST00000680710.1:c.9467A=	ENSP00000506676.1:p.Tyr3156=
ENST00000294732.11:c.4736A=	ENSP00000294732.7:p.Tyr1579=
ENST00000367408.5:c.2486A=	ENSP00000356378.1:p.Tyr829=
ENST00000367409.8:c.9491A=	ENSP00000356379.4:p.Tyr3164=
ENST00000612785.1:c.3449A=	ENSP00000479244.1:p.Tyr1150=
NM_001206846.1:c.4736A=	NP_001193775.1:p.Tyr1579=
NM_018136.4:c.9491A=	NP_060606.3:p.Tyr3164=
NM_018136.5:c.9491A= MANE Select	NP_060606.3:p.Tyr3164=
NM_001206846.2:c.4736A=	NP_001193775.1:p.Tyr1579=